2590-05-8 Usage
Uses
Used in Pharmaceutical Industry:
2-(p-Pyridyl)-Δ2-thiazolin-carbonsaeure-(4) is used as a key intermediate in the synthesis of various biologically active molecules for [application reason] its unique structural features that facilitate the development of new drugs with potential therapeutic effects.
Used in Anti-inflammatory Applications:
In the field of medicinal chemistry, 2-(p-Pyridyl)-Δ2-thiazolin-carbonsaeure-(4) is used as an anti-inflammatory agent for [application reason] its ability to modulate inflammatory pathways and reduce the associated symptoms and complications.
Used in Anti-cancer Applications:
2-(p-Pyridyl)-Δ2-thiazolin-carbonsaeure-(4) is also utilized as an anti-cancer agent for [application reason] its demonstrated potential to inhibit cancer cell growth and proliferation, making it a promising candidate for further research and development in oncology.
Used in Drug Discovery and Development:
2-(p-Pyridyl)-Δ2-thiazolin-carbonsaeure-(4) is used as a valuable tool in drug discovery and development efforts for [application reason] its chemical structure and properties that allow for the design and synthesis of novel therapeutic agents with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 2590-05-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,9 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2590-05:
(6*2)+(5*5)+(4*9)+(3*0)+(2*0)+(1*5)=78
78 % 10 = 8
So 2590-05-8 is a valid CAS Registry Number.
2590-05-8Relevant academic research and scientific papers
Predicting the reactivity of nitrile-carrying compounds with cysteine: A combined computational and experimental study
Berteotti, Anna,Vacondio, Federica,Lodola, Alessio,Bassi, Michele,Silva, Claudia,Mor, Marco,Cavalli, Andrea
supporting information, p. 501 - 505 (2014/06/09)
Here, we report on a mechanistic investigation based on DFT calculations and kinetic measures aimed at determining the energetics related to the cysteine nucleophilic attack on nitrile-carrying compounds. Activation energies were found to correlate well with experimental kinetic measures of reactivity with cysteine in phosphate buffer. The agreement between computations and experiments points to this DFT-based approach as a tool for predicting both nitrile reactivity toward cysteines and the toxicity of nitriles as electrophile agents.
